SEARCH RESULTS FOR: 怎么做假AT(5634 results)

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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Type Device Class Implantable

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PROGAV 2.0 SYS SA2.0 20 & CONTROL RES.
Aesculap AG
FX551T
In Commercial Distribution

  • 04041906503161 ()
FX551T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & CONTROL RES.
Aesculap AG
FX550T
In Commercial Distribution

  • 04041906503154 ()
FX550T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & CONTROL RES.
Aesculap AG
FX549T
In Commercial Distribution

  • 04041906503147 ()
FX549T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 35 & PRECHAMBER
Aesculap AG
FX593T
In Commercial Distribution

  • 04041906503079 ()
FX593T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 30 & PRECHAMBER
Aesculap AG
FX592T
In Commercial Distribution

  • 04041906503062 ()
FX592T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 25 & PRECHAMBER
Aesculap AG
FX591T
In Commercial Distribution

  • 04041906503055 ()
FX591T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 20 & PRECHAMBER
Aesculap AG
FX590T
In Commercial Distribution

  • 04041906503048 ()
FX590T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 15 & PRECHAMBER
Aesculap AG
FX589T
In Commercial Distribution

  • 04041906503031 ()
FX589T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS SA2.0 10 & PRECHAMBER
Aesculap AG
FX588T
In Commercial Distribution

  • 04041906503024 ()
FX588T

  • Ventriculo-peritoneal/atrial shunt
PROGAV 2.0 SYS WITH PRECHAMBER
Aesculap AG
FX587T
In Commercial Distribution

  • 04041906503017 ()
FX587T

  • Ventriculo-peritoneal/atrial shunt
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